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Maxillary Canine RetractionNCT07826182

Comparison Between Two Different Loops for Maxillary Canine Retraction

A study testing Poul Gjessing (PG) spring and Modified Marcotte spring in people with Maxillary Canine Retraction, run by Fayrouz Esam.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

The aim of the study is to evaluate and compare the clinical efficiency of two distinct loop mechanics for maxillary canine retraction, by comparing the rate of orthodontic tooth movement achieved, while assessing other dental parameters. Read more about this study

Who is it for?
Ages 16 to 25 yearsHealthy volunteers can take part
Conditions the study is for
Maxillary Canine Retraction
What is being tested?
Poul Gjessing (PG) spring and Modified Marcotte spring
Type of treatment
Medical device
Could I receive a placebo?
No, everyone receives an active treatment
How many people
20 participants
Where
No sites listed yet
Study dates
1 Sep 2026to 1 Dec 2029
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 16 to 25 years
  • All sexes
  • Healthy volunteers accepted
  • Child, Adult

Who may be able to join

  • Adults aged 16-25 years.
  • Class I or II div 1 malocclusion with moderate to severe crowding who are indicated for maxillary premolar extraction.
  • Good oral hygiene and general health.
  • Full eruption of maxillary permanent canines and second molars.

Who cannot join

  • Systemic disease affecting bone remodeling eg.DM
  • Previous extraction of permanent teeth.
  • Periodontal disease or radiographic evidence of bone loss.
  • Previous orthodontic treatment.
  • Craniofacial anomalies or cleft lip and palate.
  • Skeletal asymmetry.
  • Orthodontic cases that could be treated with no indication for extraction
  • Orthodontic cases that are indicated for extraction of any tooth other than maxillary first premolars.

Trial locations and contacts

No sites are listed yet. Contact the study team or a site near you to ask about taking part.

Fayrouz Fayrouz Esam Ahmed Taher Mahmoud contact

0201016926903

fayrouzesam17@gmail.com

About this study

Official title: Comparison Between Two Different Loops for Maxillary Canine Retraction (Split Mouth Technique)(Randomized Clinical Study)

The aim of the study is to evaluate and compare the clinical efficiency of two distinct loop mechanics for maxillary canine retraction, by comparing the rate of orthodontic tooth movement achieved, while assessing other dental parameters.

Read the detailed description

Orthodontic management of severe dental crowding and dentoalveolar protrusion frequently necessitates the extraction of maxillary first premolars. Following extraction, space closure is typically executed in a two-step procedure, initiated by isolated canine retraction to provide adequate space for subsequent incisor alignment and retraction.

Because canine retraction spans the longest duration of the space-closure phase, optimizing this stage is critical to achieving rapid, controlled tooth movement while minimizing adverse clinical effects like anchorage loss, root resorption, and unwanted tooth tipping or rotation.

In clinical orthodontics, canine retraction can be achieved through two primary biomechanical modalities: friction (sliding) mechanics and frictionless (loop/sectional) mechanics. While sliding mechanics are highly valued for their clinical simplicity, they generate significant frictional forces and binding at the bracket-arch wire interface. This friction can dissipate a substantial portion of the applied orthodontic force, cause unpredictable tooth movement and increase the risk of posterior anchorage strain. Conversely, frictionless mechanics eliminate these interface variables by utilizing specialized sectional wire loops to generate the required forces.

The success of frictionless canine retraction relies heavily on the structural design and configuration of the loop used.

Different loop designs such as the classic Burstone T-loop, the Opus loop, and the modified Marcotte spring exhibit distinct biomechanical properties:

  • Load-Deflection Rate (LDR): Determines how rapidly the force decays as the tooth moves. A lower LDR provides a safer, more constant force over time.
  • Moment-to-Force (M: F) Ratio: Governs the type of tooth movement achieved. Achieving a precise M:F ratio is mandatory to prevent uncontrolled distal tipping and promote controlled tipping or bodily movement (translation).

Despite extensive laboratory and limited element analyses detailing the theoretical behavior of various loop designs, translating these findings into real-world performance remains challenging. Individual biological variations such as; bone remodeling rates, alveolar bone density, and patient compliance introduce confounding variables that can twist clinical outcomes in traditional parallel-group clinical trials. To overcome these biological limitations, a split-mouth study design serves as an ideal methodology.

By randomly assigning different loop mechanics to opposing quadrants within the same maxillary arch of a single patient, each subject acts as their own perfectly matched control, effectively eliminating systemic biological bias. Recent clinical trials utilizing this design have started to clarify differences in loop efficiency.

For instance, comparisons between the Opus loop and the T-loop have demonstrated subtle variations in retraction rates, though both maintain comparable overall clinical performance.

Similarly, investigations contrasting the T-loop against alternative segmental systems, such as dual-force retractors or modified Marcotte springs, emphasize that loop configuration directly influences the duration of retraction, three-dimensional torque control, and the preservation of posterior anchorage.

While several clinical trials have compared sliding versus loop mechanics, head-to-head clinical comparisons evaluating efficiency, anchorage control, rotational tendencies, and patient comfort levels between different modern loop designs remain scarce. Consequently, there is an ongoing clinical debate regarding which loop configuration yields the most favorable balance between rapid canine retraction and optimal three-dimensional position control.

Being tested
Poul Gjessing (PG) spring, Modified Marcotte spring

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Poul Gjessing (PG) springDevice

    orthodontic patient treated by Poul Gjessing (PG) spring for canine retraction.

  • Modified Marcotte springDevice

    orthodontic patient treated by Modified Marcotte spring for canine retraction.

Study groups in NCT07826182
Study groupRoleWhat they receive
Poul Gjessing (PG) LoopExperimentalorthodontic patient treated by Poul Gjessing (PG) spring for canine retraction.
Receives: Device: Poul Gjessing (PG) spring
Modified Marcotte LoopExperimentalorthodontic patient treated by modified Marcotte spring for canine retraction.
Receives: Device: Modified Marcotte spring

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Maxillary Canine Retraction

    Measured: At the baseline visit (T-0), a dental impression and a CBCT scan will be obtained. For intermediate follow-up visits at months 1 through 5 (T-1 to T-5), dental impressions only will be recorded. At the final 6-month visit (T-6), both a dental impression

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted17 Sep 2026
  2. Study start1 Sep 2026 (estimated)
  3. Primary completion1 Dec 2028 (estimated)
  4. Study completion1 Dec 2029 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
20 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07826182
Sponsor's protocol ID
Canine Retraction with Loops
Status last verified
Sep 2026
First submitted
13 Sep 2026
Last updated
17 Sep 2026
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Poul Gjessing (PG) spring and Modified Marcotte spring in people with Maxillary Canine Retraction, run by Fayrouz Esam.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 8 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 17 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Fayrouz Fayrouz Esam Ahmed Taher Mahmoud (0201016926903, fayrouzesam17@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Maxillary Canine Retraction (time frame: At the baseline visit (T-0), a dental impression and a CBCT scan will be obtained. For intermediate follow-up visits at months 1 through 5 (T-1 to T-5), dental impressions only will be recorded. At the final 6-month visit (T-6), both a dental impression). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 17 Sep 2026; AzTrials last refreshed its copy on 27 Oct 2026.

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